Badii, Ramin

Publications

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selected publications

Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population. PloS one. 2018 Academic Article GET IT
Times cited: 4
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families. Mutation research. 2017 Academic Article GET IT
Times cited: 17
Correction: Type 2 Diabetes Risk Allele Loci in the Qatari Population. PloS one. 2016 Article GET IT
Times cited: 20
Type 2 Diabetes Risk Allele Loci in the Qatari Population. PloS one. 2016 Academic Article GET IT
Times cited: 20
The Qatar genome: a population-specific tool for precision medicine in the Middle East. Human genome variation. 2016 Academic Article GET IT
Times cited: 74
Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations. Genome research. 2016 Academic Article GET IT
Times cited: 62
Genetic testing and genomic analysis: a debate on ethical, social and legal issues in the Arab world with a focus on Qatar. Journal of translational medicine. 2015 Review GET IT
Times cited: 20
The Molecular Basis of α-Thalassemia in the Qatari Pediatric Population. Hemoglobin. 2015 Academic Article GET IT
Times cited: 2
The p.Cys169Tyr variant of connexin 26 is not a polymorphism. Human molecular genetics. 2015 Academic Article GET IT
Times cited: 10
Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar. Human heredity. 2015 Academic Article GET IT
Times cited: 21
Consanguinity and hereditary hearing loss in Qatar. Human heredity. 2014 Review GET IT
Times cited: 13
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients. Gene. 2014 Academic Article GET IT
Times cited: 44
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. PloS one. 2013 Academic Article GET IT
Times cited: 44
Exome sequencing identifies potential risk variants for Mendelian disorders at high prevalence in Qatar. Human mutation. 2013 Academic Article GET IT
Times cited: 41
GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population. International journal of audiology. 2011 Academic Article GET IT
Times cited: 27
Neuronal ceroid lipofuscinosis in Qatar: report of a novel mutation in ceroid-lipofuscinosis, neuronal 5 in the Arab population. Journal of child neurology. 2011 Academic Article GET IT
Times cited: 9
Lack of association between the Pro12Ala polymorphism of the PPAR-gamma 2 gene and type 2 diabetes mellitus in the Qatari consanguineous population. Acta diabetologica. 2007 Academic Article GET IT
Times cited: 26
A common mutation in the CBS gene explains a high incidence of homocystinuria in the Qatari population. Human mutation. 2006 Academic Article GET IT
Times cited: 40

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Background

education and training

Ph.D., Cranfield University (United Kingdom) 1990
B.Sc., Cardiff University (United Kingdom) 1985

Contact

full name

Ramin Badii

primary email

rab2033@qatar-med.cornell.edu

VIVO Weill Cornell Medical College

Ramin Badii Assistant Professor of Clinical Pathology and Laboratory Medicine

Publications

selected publications

Background

education and training

Contact

full name

primary email